21685-51-8 = 86906-05-0 反应条件:1.1 Reagents: Magnesium Solvents: Tetrahydrofuran; Rt1.2 8 H,Cooled1.3 Reagents: Ammonium Chloride Solvents: Water 标题:Synthesis Of Chiral Amino Alcohol Palladium(Ii) Complexes 作者:Bai,Haiyu; Et Al 参考文献:Huagong Shikan 日期:2008 卷标:22(3) 页码:5-6]
13033-84-6 = 86906-05-0 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Diethyl Ether,Water; 20 Min,Rt1.2 Solvents: Diethyl Ether; 0 °C; 0 °C -> Reflux; 9 H,Reflux 标题:Highly Diastereoselective Synthesis Of Trans-2,5-Disubstituted Tetrahydrofurans 作者:Jalce,Gael; Et Al 参考文献:Journal Of Organic Chemistry 日期:2004 卷标:69(9) 页码:3240-3241]
13033-84-6 = 86906-05-0 反应条件:1.1 Solvents: Diethyl Ether; 0 °C; 0 °C -> Rt; Overnight,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt1.3 Reagents: Sodium Hydroxide Solvents: Water; 30 Min,Rt 标题:Direct Asymmetric N-Specific Reaction Of Nitrosobenzene With Aldehydes Catalyzed By A Chiral Primary Amine-Based Organocatalyst 作者:Qin,Long; Et Al 参考文献:Chirality 日期:2011 卷标:23(7) 页码:527-533]
673-06-3 = 86906-05-0 反应条件:1.1 Reagents: Sulfuryl Chloride; 10 Min,-10 °C; 120 Min,Reflux2.1 Reagents: Sodium Hydroxide Solvents: Diethyl Ether,Water; 20 Min,Rt2.2 Solvents: Diethyl Ether; 0 °C; 0 °C -> Reflux; 9 H,Reflux 标题:Highly Diastereoselective Synthesis Of Trans-2,5-Disubstituted Tetrahydrofurans 作者:Jalce,Gael; Et Al 参考文献:Journal Of Organic Chemistry 日期:2004 卷标:69(9) 页码:3240-3241]
57728-37-7 = 86906-05-0 + 79868-78-3 反应条件:1.1 Catalysts: Palladium(2+),Bis[1,1′-(1S)-[1,1′-Binaphthalene]-2,2′-Diylbis[1,1-Diphenylphosp... Solvents: Chloroform-D; Rt 标题:Chiral Discrimination By A Binuclear Pd Complex Sensor Using 31P{1H} Nmr 作者:Chen,Zhongxiang; Et Al 参考文献:Analytical Chemistry (Washington 日期:2019 卷标:91(22) 页码:14591-14596
📜D-苯丙氨酸置于乙醚,苯基溴化镁体系中,化学反应生成 (R)-(+)-2-氨基-1,1,3-三苯基-1-丙醇 参考文献:Mckenzie; Wills,Journal Of The Chemical Society,1925,Vol. 127,P. 284 标题:Mckenzie; Wills,Journal Of The Chemical Society,1925,Vol. 127,P. 284
专利号:EP-1730108-B1 优先权日:2004-03-18 标 题:Stereoselective synthesis of vitamin d analogues 发明人:SABROE THOMAS PETER; CALVERLEY MARTIN JOHN 权利人:LEO PHARMA AS 摘要:The present invention relates to intermediates useful for the synthesis of calcipotriol or calcipotriol monohydrate, to methods of producing said intermediates, and to methods of stereoselectively reducing said intermediates.
专利号:EP-1735276-B1 优先权日:2004-04-02 标题:Novel method for the preparation of intermediates useful for the synthesis of vitamin d analogues 发明人:HANSEN ERIK TORNGAARD; SABROE THOMAS PETER; CALVERLEY MARTIN JOHN; PEDERSEN HENRIK; DEUSSEN HEINZ-JOSEF WILHELM 权利人:LEO PHARMA AS 摘要:The present invention relates to novel methods for the preparation of intermediates which are useful in the synthesis of cacipotriol. The present invention relates further to the use of intermediates produced with said methods for making calcipotriol or calcipotriol monohydrate.
专利号:US-8759555-B2 优先权日:2004-03-18 标 题:Stereoselective synthesis of vitamin D analogues 发明人:SABROE THOMAS PETER; CALVERLEY MARTIN JOHN 权利人:SABROE THOMAS PETER; CALVERLEY MARTIN JOHN; LEO PHARMA AS 摘要:The present invention relates to intermediates useful for the synthesis of calcipotriol or calcipotriol monohydrate, to methods of producing said intermediates, and to methods of stereoselectively reducing said intermediates.
专利号:RU-2378252-C2 优先权日:2004-04-02 标题 :Novel method for synthesis of intermediate compounds, used in synthesis of vitamin d analogues
专利号:US-2007027333-A1 优先权日:2004-03-18 标题 :Stereoselective synthesis of vitamin d analogues
专利号:CA-2555260-C 优先权日:2004-03-18 标 题 :Stereoselective synthesis of vitamin d analogues
参考标题:Direct Asymmetric N-Specific Reaction Of Nitrosobenzene With Aldehydes Catalyzed By A Chiral Primary Amine-Based Organocatalyst 作者:Long Qin,Lei Li,Lei Yi,Chao-Shan Da,Yi-Feng Zhou |发布日期:2011.8 摘要:Interesting And Important To Perform A Nitrogen Or Oxygen Selective Reaction With Interesting Substrates. These Atom Specific Reactions Are Crucial To Specifically Synthesis Of Specific Compounds. An Enantioselective N‐specific Reaction Of Nitrosobenzene With Unmodified Aldehydes Was Successfully Achieved Catalyzed First By A Variety Of Primary Amine‐based Organocatalysts With Higher Yield And Enantioselectivity